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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57501생성일: 2026년 10월 23일

Nitrogen → tert-butyl (S)-(1-(4-methyl-2'-(trifluoromethyl)-[3,4'-bipyridin]-6-yl)ethyl)carbamate

https://huagongshe.com/ko/reaction/57501

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Sodium CarbonateHCID 10340—
반응물2-(Trifluoromethyl)pyridine-4-boronic acidHCID 45158880—
반응물(S)-tert-butyl (1-(5-bromo-4-methylpyridin-2-yl)ethyl)carbamateHCID 90451674—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl (S)-(1-(4-methyl-2'-(trifluoromethyl)-[3,4'-bipyridin]-6-yl)ethyl)carbamateHCID 9045168782.6%

반응 조건

온도90 °C

반응 단계

N2 was bubbled through a solution of (S)-tert-butyl(1-(5-bromo-4-methylpyridin-2-yl)ethyl)carbamate (200 mg, 0.635 mmol), (2-(trifluoromethyl)pyridin-4-yl)boronic acid (145 mg, 0.761 mmol) and Na2CO3 (2.0 M, 635 μl, 1.269 mmol) in dioxane for 5 min. Cl2Pd(dppf) (CH2Cl2 adduct) (51.8 mg, 0.063 mmol) was added. The reaction mixture was stirred at 90° C. for 16 hr. The mixture was diluted with EtOAc, washed with water, brine, dried over Na2SO4, filtered, concentrated and purified through flash column chromatography (0-100% EtOAc/Heptane) to give 200 mg (S)-tert-butyl(1-(4-methyl-2′-(trifluoromethyl)-[3,4′-bipyridin]-6-yl)ethyl)carbamate as a white solid. 1H NMR (400 MHz, CDCl3) δ 8.83 (d, J=4.9 Hz, 1H), 8.36 (s, 1H), 7.66 (s, 1H), 7.51-7.42 (m, 1H), 7.21 (s, 1H), 5.60 (d, J=7.7 Hz, 1H), 4.87 (p, J=6.9 Hz, 1H), 2.30 (s, 3H), 1.48 (d, J=6.9 Hz, 3H), 1.45 (s, 9H). MS m/z 382.3 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434719B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-98e2c8b0f4f348fd901f5a2a1e05f29b
출처 메모uspto-grants-2016_09